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NPJ Vaccines . SARS-CoV-2 ferritin nanoparticle vaccine induces robust innate immune activity driving polyfunctional spike-specific T cell responses

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  • NPJ Vaccines . SARS-CoV-2 ferritin nanoparticle vaccine induces robust innate immune activity driving polyfunctional spike-specific T cell responses


    NPJ Vaccines


    . 2021 Dec 13;6(1):151.
    doi: 10.1038/s41541-021-00414-4.
    SARS-CoV-2 ferritin nanoparticle vaccine induces robust innate immune activity driving polyfunctional spike-specific T cell responses


    Joshua M Carmen # 1 , Shikha Shrivastava # 1 2 , Zhongyan Lu # 3 , Alexander Anderson 1 4 , Elaine B Morrison 1 , Rajeshwer S Sankhala 5 6 , Wei-**** Chen 5 6 , William C Chang 5 6 , Jessica S Bolton 7 , Gary R Matyas 1 , Nelson L Michael 8 , M Gordon Joyce 5 6 , Kayvon Modjarrad 5 , Jeffrey R Currier 9 , Elke Bergmann-Leitner 7 , Allison M W Malloy 10 , Mangala Rao 11



    Affiliations

    Abstract

    The emergence of variants of concern, some with reduced susceptibility to COVID-19 vaccines underscores consideration for the understanding of vaccine design that optimizes induction of effective cellular and humoral immune responses. We assessed a SARS-CoV-2 spike-ferritin nanoparticle (SpFN) immunogen paired with two distinct adjuvants, Alhydrogel® or Army Liposome Formulation containing QS-21 (ALFQ) for unique vaccine evoked immune signatures. Recruitment of highly activated multifaceted antigen-presenting cells to the lymph nodes of SpFN+ALFQ vaccinated mice was associated with an increased frequency of polyfunctional spike-specific memory CD4+ T cells and Kb spike-(539-546)-specific long-lived memory CD8+ T cells with effective cytolytic function and distribution to the lungs. The presence of this epitope in SARS-CoV, suggests that generation of cross-reactive T cells may be induced against other coronavirus strains. Our study reveals that a nanoparticle vaccine, combined with a potent adjuvant that effectively engages innate immune cells, enhances SARS-CoV-2-specific durable adaptive immune T cell responses.


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